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5 jobs found in totowa, new jersey

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    • parsippany, new jersey
    • contract
    • $18 - $23.94 per hour
    job summary: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!   location: Parsippany, New Jersey job type: Contract salary: $18.00 - 23.94 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Provides analytical support to client groups.Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes early stage prototypes, lab samples, pilot plant samples, production samples, stability samples and competitor samples. Possesses extensive knowledge of various laboratory instruments like HPLC, GC, AA, Dissolution, IC, etc.  qualifications: MUST HAVE 1-3 years lab experienceBachelor Degree in Chem or Science is a must MS= okay as well Ideal: Chemistry 2 - 4 Years empower 3 software 2 - 4 Years  skills: HPLC, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!   location: Parsippany, New Jersey job type: Contract salary: $18.00 - 23.94 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Provides analytical support to client groups.Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes early stage prototypes, lab samples, pilot plant samples, production samples, stability samples and competitor samples. Possesses extensive knowledge of various laboratory instruments like HPLC, GC, AA, Dissolution, IC, etc.  qualifications: MUST HAVE 1-3 years lab experienceBachelor Degree in Chem or Science is a must MS= okay as well Ideal: Chemistry 2 - 4 Years empower 3 software 2 - 4 Years  skills: HPLC, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • ridgefield, new jersey
    • contract
    • $23 - $28.57 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Ridgefield, New Jersey job type: Contract salary: $23.00 - 28.57 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Tasks to be completed may include fermentation, protein purification, solvent extractions, tissue culture, preparation of bulk solutions, aseptic fills of buffers, filling and labeling of vials under sterile and non-sterile conditions, routine buffer and media preparation, filtration, vial preparation and sterilization.Operate general manufacturing equipment in strict accordance with SOPs to complete tasks as noted above as well as large scale bioreactor operations, critical small or large volume sterile fills, and aseptic manipulation of cell cultures.Operate with minimal supervision complex systems and equipment and optimizes their use in accordance with defined goals.May participate in plant trials for evaluating process modifications.Troubleshoot processing problems.Assist in the implementation of production procedures to optimize manufacturing processes.May attend research meetings related to the transfer process of new products.May prepare monthly operating reports for use in the analysis of the performance of the unit.Participate in authoring complex, explicit documentation for manufacturing operations.May provide training to new personnel in a specific technical process.Demonstrated ability in the application of requisite skills and applies additional skills and knowledge acquired through experience to perform the more complex tasks of the position.Generally receive no instructions on routine assignments while under little or no supervision.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.Requires physical demands of lifting up to 30 lbs/14 kg to 35 lbs/16 kg.The work environment characteristics described here are representative of those an employee to encounters while performing the essential functions of this job.Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.May involve work with hazardous materials.  qualifications: - Must have B.S. degree in science or equivalent. - 3-6 years' work experience required. - Requires Good Documentation Skills - Requires Attention to Detail   skills: SOP, MS-WORD, MS-EXCEL, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Ridgefield, New Jersey job type: Contract salary: $23.00 - 28.57 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Tasks to be completed may include fermentation, protein purification, solvent extractions, tissue culture, preparation of bulk solutions, aseptic fills of buffers, filling and labeling of vials under sterile and non-sterile conditions, routine buffer and media preparation, filtration, vial preparation and sterilization.Operate general manufacturing equipment in strict accordance with SOPs to complete tasks as noted above as well as large scale bioreactor operations, critical small or large volume sterile fills, and aseptic manipulation of cell cultures.Operate with minimal supervision complex systems and equipment and optimizes their use in accordance with defined goals.May participate in plant trials for evaluating process modifications.Troubleshoot processing problems.Assist in the implementation of production procedures to optimize manufacturing processes.May attend research meetings related to the transfer process of new products.May prepare monthly operating reports for use in the analysis of the performance of the unit.Participate in authoring complex, explicit documentation for manufacturing operations.May provide training to new personnel in a specific technical process.Demonstrated ability in the application of requisite skills and applies additional skills and knowledge acquired through experience to perform the more complex tasks of the position.Generally receive no instructions on routine assignments while under little or no supervision.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.Requires physical demands of lifting up to 30 lbs/14 kg to 35 lbs/16 kg.The work environment characteristics described here are representative of those an employee to encounters while performing the essential functions of this job.Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.May involve work with hazardous materials.  qualifications: - Must have B.S. degree in science or equivalent. - 3-6 years' work experience required. - Requires Good Documentation Skills - Requires Attention to Detail   skills: SOP, MS-WORD, MS-EXCEL, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • whippany, new jersey (remote)
    • contract
    • $42.85 - $50.41 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $42.85 - 50.41 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. DEPARTMENT/TEAM DESCRIPTION Operational Excellence and Project Management in Global Medical Affairs (GMA), Oncology SBU is a global function which partners and collaborates with the MA Teams and Key Stakeholders (internal and external) to assist in achieving short and long term strategic goals while adhering to "LIFE" values (leadership, integrity, flexibility, efficiency). POSITION SUMMARY The Senior Contract Operations Excellence & PM Manager position is accountable for compliant and high quality management of GMA company-sponsored studies (both non and interventional), Investigator Initiated Research (IIR) and Investigator-Sponsored Collaborative Studies (ISCS) data acquisition projects, and Expanded Access Programs (EAPs) POSITION DUTIES & RESPONSIBILITIES Lead all aspects of clinical studies from planning to execution. Assigned studies include interventional, non-interventional and data acquisitions within Global Medical Affairs Oncology SBUOverall accountable for study management of assigned studies, serve as primary contact for CRO. Lead and manage multi-disciplinary cross functional team in all aspects of studies activities including but not limited to site start up, CRO/vendor selection and management, study-specific timelines and study executionCoordinate for fair market value assessment of study budgets; initiate and manage contracting process. Liaise with appropriate internal protocol review committees to ensure timely review, response and finalization of the protocol and protocol amendmentIIR and/or ISCS data acquisition projects. Responsibilities include chair conference calls, coordinate between team and IIR-sponsors on activities such as data review, query resolution and independent review of imaging scans, when applicable. Develop and manage overall project timelinesSupport GMA Medical Leads on overall delivery of the data generated from Oncology Non-Interventional Studies (NIS). Responsibilities include, but not limited to, monitor country/site selection and activation process, contribute in CRF design and review, study budget management, support Medical Leads on clinical data consistency review to ensure that data issues raised during medical and DM data review are adequately queried and resolvedManage study drug forecasting. Liaise with Clinical Supplies Management to ensure drug supply planning, labeling and distribution are executed timely and within applicable country and regional guidelinesAssist and/or lead in executing Expanded Access Programs within Oncology MA. Responsibilities include collaborate with country affiliates and Medical Experts as appropriate to ensure timely alignment and execution of country specific processes including permit license application, commercial product transition plan, and Real World Data (RWD) data generation when applicable  qualifications: SKILLS Extensive (7+ years) study management experience involving Phases 2 & 3 studies from planning through regulatory submission; regulatory submission experience a plusUnderstanding of the connection between protocol endpoints, study design, CRF design and data collection; clinical science backyard a plusAt least 5 years Oncology experience (can be outside of industry)Strong written, organizational, and computer (e.g. Excel, power point) skillsExcellent interpersonal and communication skills as candidate will interact with cross functional team members as well as liaise with external academic networks and cooperative groups from all over the global Preferences: Medical Affairs experience preferred REQUIREMENTS/PREFERENCES Education Requirement(s): Bachelor's degree required; life science preferredMasters in Science or Business Administration - preferred  skills: MS-EXCEL, Study Planning Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $42.85 - 50.41 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. DEPARTMENT/TEAM DESCRIPTION Operational Excellence and Project Management in Global Medical Affairs (GMA), Oncology SBU is a global function which partners and collaborates with the MA Teams and Key Stakeholders (internal and external) to assist in achieving short and long term strategic goals while adhering to "LIFE" values (leadership, integrity, flexibility, efficiency). POSITION SUMMARY The Senior Contract Operations Excellence & PM Manager position is accountable for compliant and high quality management of GMA company-sponsored studies (both non and interventional), Investigator Initiated Research (IIR) and Investigator-Sponsored Collaborative Studies (ISCS) data acquisition projects, and Expanded Access Programs (EAPs) POSITION DUTIES & RESPONSIBILITIES Lead all aspects of clinical studies from planning to execution. Assigned studies include interventional, non-interventional and data acquisitions within Global Medical Affairs Oncology SBUOverall accountable for study management of assigned studies, serve as primary contact for CRO. Lead and manage multi-disciplinary cross functional team in all aspects of studies activities including but not limited to site start up, CRO/vendor selection and management, study-specific timelines and study executionCoordinate for fair market value assessment of study budgets; initiate and manage contracting process. Liaise with appropriate internal protocol review committees to ensure timely review, response and finalization of the protocol and protocol amendmentIIR and/or ISCS data acquisition projects. Responsibilities include chair conference calls, coordinate between team and IIR-sponsors on activities such as data review, query resolution and independent review of imaging scans, when applicable. Develop and manage overall project timelinesSupport GMA Medical Leads on overall delivery of the data generated from Oncology Non-Interventional Studies (NIS). Responsibilities include, but not limited to, monitor country/site selection and activation process, contribute in CRF design and review, study budget management, support Medical Leads on clinical data consistency review to ensure that data issues raised during medical and DM data review are adequately queried and resolvedManage study drug forecasting. Liaise with Clinical Supplies Management to ensure drug supply planning, labeling and distribution are executed timely and within applicable country and regional guidelinesAssist and/or lead in executing Expanded Access Programs within Oncology MA. Responsibilities include collaborate with country affiliates and Medical Experts as appropriate to ensure timely alignment and execution of country specific processes including permit license application, commercial product transition plan, and Real World Data (RWD) data generation when applicable  qualifications: SKILLS Extensive (7+ years) study management experience involving Phases 2 & 3 studies from planning through regulatory submission; regulatory submission experience a plusUnderstanding of the connection between protocol endpoints, study design, CRF design and data collection; clinical science backyard a plusAt least 5 years Oncology experience (can be outside of industry)Strong written, organizational, and computer (e.g. Excel, power point) skillsExcellent interpersonal and communication skills as candidate will interact with cross functional team members as well as liaise with external academic networks and cooperative groups from all over the global Preferences: Medical Affairs experience preferred REQUIREMENTS/PREFERENCES Education Requirement(s): Bachelor's degree required; life science preferredMasters in Science or Business Administration - preferred  skills: MS-EXCEL, Study Planning Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • south plainfield, new jersey
    • contract
    • $40 - $45 per hour
    job summary: The Research Biologist is responsible for performing scientific experiments that contribute to Research and Drug discovery activities. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team.   location: South Plainfield, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under direct supervision, executes experiments and communicates results as part of multi-disciplinary team(s).Applies relevant scientific principles and techniques to research problems.Maintains detailed laboratory notebooks.Abides by all safety requirements.Ability to trouble shoot experimentsContributes to general laboratory needs/operation.Specific duties may also include, but may not be limited to, the following:Provides support for the characterization of compounds on different immune cells.Provides support for lead optimization by screening compounds and/or supporting structure activity relationship (SAR) studies involving the characterization of the biological activity of compounds in various assays. Profiles selected compounds in additional cells/assays.Provides support for in vitro studies as required.Assists in the development of biologically relevant preclinical animal models.  qualifications: Bachelor's degree in a scientific discipline with at least 3 years of research experience. Master's degree preferred.Hands-on experience in mammalian cell culture, and various cell-based assay technologies, such as CellTiterGlo, ELISA and HTRF.Knowledge of and ability to use standard cell biology and molecular biology techniques including western blotting, RT-PCR, qPCR and data analysis.Proficiency with Microsoft Office- preferably MS Excel and MS PowerPoint, and Graphpad Prism.Ability to work collaboratively under direct supervision, in a fast-paced, matrixed, team environment.Excellent planning, organization, and time management skills.Effective verbal and written communication and skills. Preferred: Experience performing transient and stable transfection, Lentiviral transduction, RNAi or CRISPR assays is desired.Compound screening in 96-well or 384-well format is a strong plus.?Immunofluorescence microscopy is a plus.  skills: Cell Biology, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Research Biologist is responsible for performing scientific experiments that contribute to Research and Drug discovery activities. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team.   location: South Plainfield, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under direct supervision, executes experiments and communicates results as part of multi-disciplinary team(s).Applies relevant scientific principles and techniques to research problems.Maintains detailed laboratory notebooks.Abides by all safety requirements.Ability to trouble shoot experimentsContributes to general laboratory needs/operation.Specific duties may also include, but may not be limited to, the following:Provides support for the characterization of compounds on different immune cells.Provides support for lead optimization by screening compounds and/or supporting structure activity relationship (SAR) studies involving the characterization of the biological activity of compounds in various assays. Profiles selected compounds in additional cells/assays.Provides support for in vitro studies as required.Assists in the development of biologically relevant preclinical animal models.  qualifications: Bachelor's degree in a scientific discipline with at least 3 years of research experience. Master's degree preferred.Hands-on experience in mammalian cell culture, and various cell-based assay technologies, such as CellTiterGlo, ELISA and HTRF.Knowledge of and ability to use standard cell biology and molecular biology techniques including western blotting, RT-PCR, qPCR and data analysis.Proficiency with Microsoft Office- preferably MS Excel and MS PowerPoint, and Graphpad Prism.Ability to work collaboratively under direct supervision, in a fast-paced, matrixed, team environment.Excellent planning, organization, and time management skills.Effective verbal and written communication and skills. Preferred: Experience performing transient and stable transfection, Lentiviral transduction, RNAi or CRISPR assays is desired.Compound screening in 96-well or 384-well format is a strong plus.?Immunofluorescence microscopy is a plus.  skills: Cell Biology, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • tarrytown, new york
    • contract
    • $75 - $77 per hour
    job summary: Job Description: We are looking for a Senior Manager, Project Management who is responsible for providing project leadership and support to the sponsors, initiative leads and team members of assigned cross-functional strategic non-study initiatives. Projects are to deliver results per charter goals, on time and with good quality. They will support initiatives throughout the project from conceptualization through implementation phases as applicable. This individual will also provide subject-matter expertise to further develop the PMO maturation as advised by Director, Project Management. They will collaborate and interact with Global Development senior staff, assigned initiative leads, and initiative-specific cross-functional partners.   location: Tarrytown, New York job type: Contract salary: $75 - 77 per hour work hours: 9 to 5 education: Bachelors   responsibilities: A typical day may include the following: Lead cross functional project teams to ensure successful execution of team strategies and project plans to drive quality outcomes mapped to strategy. Responsible for planning, organizing, and assigning project responsibilities for the completion of Global Development's and our clients goals. Guide teams through creation, management approval, execution, and termination/closeout of project plans. Define the scope of the project in collaboration with Senior Leadership Gather and document requirements from key partners Build a detailed work plan which identifies and sequences the activities needed to successfully complete the project Determine the resources (time, money, people, etc) required to complete the project and work with business leaders to ensure the appropriate resources are allocated to the project Develop a schedule for project completion that effectively allocates the resources to the activities Review the project schedule with senior management and all other staff that will be affected by the project activities; revise the schedule as required and communicate project risks Determine the objectives and measures upon which the project will be evaluated at its completion Collaborate effectively with functional areas, support functions to facilitate project delivery, identifies constraints and potential workarounds where necessary Leverage relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results. Support Project Sponsors to advocate for the project and it's outcomes Provide company organizational and process expertise to enable teams to navigate development, governance and business requirements. Ensure project schedules and risk management plans are fully developed and updated and communications within and from the team are clear and effective. Prepare regular reports that summarize project status/issues and documents/presentations for senior management/governance committees Maintain accurate project data in enterprise project management systems and databases. Prepare for, facilitate, and document outcomes of team meetings, ensuring meetings have clear purpose and objectives and that conflict is surfaced and resolved. Evaluate the outcomes of the project as established during the planning phase Monitor project performance against scope, schedule, and cost baselines Collaborate closely with CM to establish a communication schedule to update partners including appropriate staff in the organization on the progress of the project Review the quality of the work completed with the project team on a regular basis to ensure that it meets the project standards Lead projects to support the PMOs maturation Apply junior project manager support to deliver administrative aspects of projects (as available)  qualifications: This job may be for you if you have: Excellent verbal and written communication and organizational skills. Strong analytical capabilities. Able to interact with and influence partners across a highly matrixed organization. Manage complex projects under agreed deadlines. Listening and responding to collaborator needs (internal and external) to enable GD project outcomes. Build and use relationships across organizational boundaries and levels within Regeneron. Able to adapt and respond quickly as required. Experience working on Diversity, Equity & Inclusion Initiatives Customer Focus Stakeholder Partnership Knowledge Management Project & Change Management Entrepreneurship Conflict Management  skills: Clinical Study Design Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Job Description: We are looking for a Senior Manager, Project Management who is responsible for providing project leadership and support to the sponsors, initiative leads and team members of assigned cross-functional strategic non-study initiatives. Projects are to deliver results per charter goals, on time and with good quality. They will support initiatives throughout the project from conceptualization through implementation phases as applicable. This individual will also provide subject-matter expertise to further develop the PMO maturation as advised by Director, Project Management. They will collaborate and interact with Global Development senior staff, assigned initiative leads, and initiative-specific cross-functional partners.   location: Tarrytown, New York job type: Contract salary: $75 - 77 per hour work hours: 9 to 5 education: Bachelors   responsibilities: A typical day may include the following: Lead cross functional project teams to ensure successful execution of team strategies and project plans to drive quality outcomes mapped to strategy. Responsible for planning, organizing, and assigning project responsibilities for the completion of Global Development's and our clients goals. Guide teams through creation, management approval, execution, and termination/closeout of project plans. Define the scope of the project in collaboration with Senior Leadership Gather and document requirements from key partners Build a detailed work plan which identifies and sequences the activities needed to successfully complete the project Determine the resources (time, money, people, etc) required to complete the project and work with business leaders to ensure the appropriate resources are allocated to the project Develop a schedule for project completion that effectively allocates the resources to the activities Review the project schedule with senior management and all other staff that will be affected by the project activities; revise the schedule as required and communicate project risks Determine the objectives and measures upon which the project will be evaluated at its completion Collaborate effectively with functional areas, support functions to facilitate project delivery, identifies constraints and potential workarounds where necessary Leverage relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results. Support Project Sponsors to advocate for the project and it's outcomes Provide company organizational and process expertise to enable teams to navigate development, governance and business requirements. Ensure project schedules and risk management plans are fully developed and updated and communications within and from the team are clear and effective. Prepare regular reports that summarize project status/issues and documents/presentations for senior management/governance committees Maintain accurate project data in enterprise project management systems and databases. Prepare for, facilitate, and document outcomes of team meetings, ensuring meetings have clear purpose and objectives and that conflict is surfaced and resolved. Evaluate the outcomes of the project as established during the planning phase Monitor project performance against scope, schedule, and cost baselines Collaborate closely with CM to establish a communication schedule to update partners including appropriate staff in the organization on the progress of the project Review the quality of the work completed with the project team on a regular basis to ensure that it meets the project standards Lead projects to support the PMOs maturation Apply junior project manager support to deliver administrative aspects of projects (as available)  qualifications: This job may be for you if you have: Excellent verbal and written communication and organizational skills. Strong analytical capabilities. Able to interact with and influence partners across a highly matrixed organization. Manage complex projects under agreed deadlines. Listening and responding to collaborator needs (internal and external) to enable GD project outcomes. Build and use relationships across organizational boundaries and levels within Regeneron. Able to adapt and respond quickly as required. Experience working on Diversity, Equity & Inclusion Initiatives Customer Focus Stakeholder Partnership Knowledge Management Project & Change Management Entrepreneurship Conflict Management  skills: Clinical Study Design Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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